Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 2 2018 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 1 2012 2012
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.710 1.000 1 2013 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.730 1.000 1 2013 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 3 2011 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0011847
Disease: Diabetes
Diabetes
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0018801
Disease: Heart failure
Heart failure
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
High density lipoprotein measurement
0.800 1.000 11 2009 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.830 1.000 2 2010 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
Low density lipoprotein cholesterol measurement
0.800 1.000 6 2010 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.810 1.000 1 2012 2012
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
Platelet Component Distribution Width Measurement
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016